AbstractAbstract 3401 Background:Early identification of children with deep venous thrombosis (DVT) of the limb, whoare at heightened risk for post-thrombotic syndrome (PTS), is important in order to evaluate therapeutic interventions aimed at decreasing the risk and severity of PTS. Objective:We sought to evaluate prognostic factors for PTS in children following DVT of the limbs. Methods:In this bi-institutional mixed cohort study with prospective ascertainment of PTS using a validated pediatric instrument, we collected data on patient/thrombus characteristics, thrombophilia testing results, and outcomes in children (<21 years at event) diagnosed with acute limb DVT at Rady Children’s Hospital of San Diego and Children’s Hospital Colorado. Results:Median age at presentation was 13 years (range, 0–18 years). Cumulative incidence (i.e., risk of PTS) was 23%, at a median follow-up duration of 33 months (range: 13.2–65 months). The presence of a lupus anticoagulant by dilute Russell Viper venom time (dRVVT) testing within two weeks of DVT diagnosis was associated with markedly increased odds of developing clinically-significant PTS (OR 16.8, 95%CI (1.60–176.2); P=0.02). The presence of an infectious or inflammatory condition at DVT presentation was neither associated with PTS risk nor dRVVT positivity. Conclusions:An acutely positive dRVVT following diagnosis of limb DVT appears to be a significant prognostic factor for development of clinically significant PTS in children. Larger collaborative cohort studies are required to substantiate these findings, evaluate other prognostic factors, and determine whether the present association is modulated by persistent dRVVT positivity or beta-2-glycoprotein-I dependence.Table 1Patient CharacteristicsVariableDVT events n=35Clinically Significant PTS n=8No Clinically Significant PTS n=27P valueAge (year)Median1315.5100.06Range0.2–180.6–170.2–18Gender (%)0.41Male22 (63)4 (50)18 (67)Female13 (37)4 (50)9 (33)BMI %Median73.168.7576.450.48Range0.1–99.80.1–9618.9–99.8Clinical Characteristics (%)Central Line Associatedà14 (40)2 (25)12 (44)0.43Infection/Inflammatory ConditionÆ14 (40)3 (38)11 (41)1.00Laboratory ParametersFV Leiden Heterozygote – (%)7 (20)2 (25)5 (19)1.00FV Leiden Homozygote – (%)1 (3)1 (13)0 (0)0.23FII G20210A heterozygote– no. tested (%)0/34 (0)0/8 (0)0/26 (0)1.00Moderate/Severe protein C, protein S, or AT deficiency – no. tested (%)3/30 (10)0/7 (0)3/23 (13)1.00FVIII Level (IU/dL)(n=19)(n =4)(n=15)Median (n =23)221A226.52080.55Range99.9–413.7215.9–295.599.9–413.7dRVVT – no. positive/tested (%)11/26 (42)6/7 (86)5/19 (26)0.02D-dimer > 500 ng/mL (%)20/26 (77)6/6 (100)14/20 (70)0.28Veno-Occlusion at Diagnosis (%)23 (66)8 (100)15 (56)0.03Veno-Occlusion 3 months after diagnosis (%)7 (20)2 (25)5 (19)0.65Recurrent VTE (%)7 (20)2 (25)5 (19)0.65Follow-Up (months)Median3340300.27Range13.2–6519–6013–65àCentral line at time of VTE or within the preceding 30 days.ÆInflammatory/Infectious Conditions include acute infection (sepsis n=2, influenza n=2, pneumonia n=2, viral encephalitis n=1, osteomyelitis n=1, necrotizing enterocolitis n=1, CNS tuberculosis n=1), inflammatory bowel disease n=1, hemolytic uremic syndrome n=2, diabetic ketoacidosis n=1, systemic lupus erythematosus n= 1, anti-NMDA receptor encephalitis n= 1, malignancy n=1 (Several subjects with > 1 disorder).Table 2Univariate Logistic Regression Analysis of Prognostic Factors for Clinically-Significant PTS* Following Diagnosis of VTEPrognostic FactorUnivariate Odds Ratio (95% CI)P valueAge1.15 (0.96–1.38)0.12BMI0.99 (0.96–1.02)0.38Gender0.50 (0.10–2.48)0.40Central Line0.42 (0.07–2.45)0.33Veno-Occlusion at Diagnosis4.15 (0.42–40.6)0.22Proximal DVT0.88 (0.08–9.79)0.91Inflammatory or Infectious condition0.87 (0.17–4.43)0.87FVIII1.00 (0.99–1.02)0.78dRVVT16.8 (1.60–176.2)0.02D-dimer > 500 ng/mL2.14 (0.2–22.5)0.53Inherited thrombophilia#1.72 (0.32–9.10)0.53*Score > 1 in both physical examination and functional limitation categories, according to the Manco-Johnson instrument, a standardized PTS assessment tool.#Presence of one or more of the following: factor V Leiden polymorphism, factor II G20210A polymorphism, or plasma protein C activity < 40%; plasmas free protein S antigen level <40%, or plasma antithrombin activity < 60% after 6 months of age. [Display omitted] Disclosures:Goldenberg:Eisai Inc: Research Funding; Pfizer Inc: Membership on an entity's Board of Directors or advisory committees; CPC Clinical Research: Consultancy.